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#620501 - ZIEGLER-HUANG SYNDROME; ZHS
Cytogenetic locations: #####
Gene summaries Genetic tests Medical literature
*619600 - AMINOPEPTIDASE O; AOPEP
Cytogenetic locations: @s####
#619565 - DYSTONIA 31; DYT31
*619411 - SIGNAL PEPTIDASE COMPLEX, SUBUNIT 2; SPCS2
Cytogenetic locations: coamplified
#619326 - BDV SYNDROME; BDVS
Cytogenetic locations: ###;##
#619306 - NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND CEREBELLAR HYPOPLASIA; NEDFACH
#619076 - NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND BRAIN ATROPHY; NEDMISB
Cytogenetic locations: between
#619072 - NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND BRAIN ATROPHY; NEDSEBA
#618858 - DIABETES MELLITUS, PERMANENT NEONATAL, 4; PNDM4
Cytogenetic locations: 11p15.5
*618854 - SIGNAL PEPTIDASE COMPLEX, SUBUNIT 3; SPCS3
Cytogenetic locations: ########aH##
#618760 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS; NEDHAHM
*618258 - SEC11 HOMOLOG A, SIGNAL PEPTIDASE COMPLEX SUBUNIT; SEC11A
Cytogenetic locations: 603773
#617936 - BUTYRYLCHOLINESTERASE DEFICIENCY; BCHED
SUXAMETHONIUM SENSITIVITY, INCLUDED
#617921 - AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 25; ALS25
#617572 - EXUDATIVE VITREORETINOPATHY 7; EVR7
Cytogenetic locations: 0#####
#617235 - MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY
Cytogenetic locations: py####
#617024 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H; CSNB1H
Cytogenetic locations: p#%###
#617018 - SPINOCEREBELLAR ATAXIA 43; SCA43
Cytogenetic locations: #s####
#617017 - CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T; CMT2T
Cytogenetic locations: #Tw]##
#616214 - HYPERPROINSULINEMIA
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